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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ST Internal Implant System
Megagen Implant Co. Ltd
ST4511D
In Commercial Distribution

  • 08809985651267 ()
ST4511DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4510D
In Commercial Distribution

  • 08809985651250 ()
ST4510DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4508D
In Commercial Distribution

  • 08809985651243 ()
ST4508DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4507D
In Commercial Distribution

  • 08809985651236 ()
ST4507DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4015D
In Commercial Distribution

  • 08809985651229 ()
ST4015DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4013D
In Commercial Distribution

  • 08809985651212 ()
ST4013DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4011D
In Commercial Distribution

  • 08809985651205 ()
ST4011DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4010D
In Commercial Distribution

  • 08809985651199 ()
ST4010DC

  • Screw endosteal dental implant, two-piece
ST Internal Implant System
Megagen Implant Co. Ltd
ST4008D
In Commercial Distribution

  • 08809985651182 ()
ST4008DC

  • Screw endosteal dental implant, two-piece
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution

  • 04047844114247 ()

  • 16x10x32mm
TST20161032

  • Metallic spinal interbody fusion cage
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